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A healthier future. Its what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. Thats what makes us Roche.
This role is within Biostatistics a core function within Product Development Data Science and Analytics (PDD) that provides strategic leadership and scientific rigor across Development at Roche. Biostatistics identifies opportunities to apply the full breadth of data digital and design capabilities to deploy innovative methods across PDD PD and the broader Roche Pharma organization.
As trusted analytical partners in end-to-end drug development Biostatistics leverages data to drive scientifically rigorous programmatic decisions across Roches Development portfolio; Biostatistics designs robust trials and analysis plans that increase the probability of technical success accelerating timelines to advance Roches clinical pipeline and promote regulatory success ultimately bringing medicines to our patients faster.
The Opportunity:
This Statistician internship role will support the statistician in clinical trials. The statistician is a key member of the cross-functional study or molecule team responsible for applying statistical expertise to the design conduct analysis and interpretation of individual clinical trials. ensures the scientific rigor and regulatory compliance of the study by contributing to protocol development authoring statistical analysis plans performing or overseeing data analyses and supporting the interpretation and communication of results. The Statistician plays a critical role in ensuring that each study generates robust meaningful data to support decision-making and regulatory submissions. The internship will provide opportunities to learn and contribute in some of the following statistician responsibilities:
Contribute to trial design under guidance applying standard statistical methods
Draft and review protocols statistical analysis plans (SAPs) and case report forms (CRFs) using templates and precedents
Perform or support statistical analyses as per statistical analysis plans escalating issues when needed
Collaborate with study team members to meet deliverables following existing processes
Summarize findings clearly with support from senior colleagues
contribute to CSR development and regulatory responses using established templates
Apply judgment to address moderately complex statistical or data issues balancing scientific rigor with appropriate flexibility and seek guidance when facing novel or ambiguous situations
Adhere to functional standards by participating in peer review and mentoring relationships to uphold quality and build methodological and regulatory expertise
Who You Are:
You are currently enrolled in a graduate program for an MSc or PhD in Statistics Biostatistics or a closely related quantitative field
You have a strong understanding of statistical principles and methodology relevant to clinical trial design and analysis
You are proficient in SAS and/or R
You demonstrate capacity for independent thinking and ability to make decisions based upon sound principles
You bring excellent strategic agility including problem-solving and critical thinking skills and agility that extends beyond the technical domain
You demonstrate respect for cultural differences when interacting with colleagues in the global workplace
You have excellent verbal and written communication skills specifically in the areas of presentation and writing with the ability to explain complex technical concepts in clear language.
A curious and proactive learner who stays engaged with the evolving landscape of data science and is dedicated to continuous professional development.
Preferred:
Experience working in cross-functional teams
Effective communication skills with the ability to translate complex statistical concepts for non-statistical audiences
Experience with multiple phases of drug development (early and/or late stage)
Excellent communication skills including the ability to influence and translate complex data for non-technical stakeholders
Strategic mindset with the ability to contribute to portfolio-level decisions
Additional Information:
Location: Based in Mississauga Hybrid (majority of days in the office).
Hours: Full-time (35 hours per week) Internship
Length: This position is an 8 or 12 month internship and is expected to begin in May 2026.
Multiple openings.
This position is not eligible for relocation support.
#RocheInternshipCA2026
The expected salary range for this position based on the primary location of Mississauga isandof hiring range. Actual pay will be determined based on experience qualifications and other job-related factors as determined by the company.We use artificial intelligence to screen assess or select applicants for this role.
This posting is for an existing vacancy at Hoffmann-La Roche Ltd.
A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver life-changing healthcare solutions that make a global impact.
Lets build a healthier future together.
Roche is an Equal Opportunity Employer.
Required Experience:
Intern
F. Hoffmann-La Roche AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel.